Canonical Allele Identifier: CA2648593748

Gene: CRP

Linked Data

• gnomAD v4: 1-159713697-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.159713699del , CM000663.2:g.159713699del	GRCh38
NC_000001.10:g.159683489del , CM000663.1:g.159683489del	GRCh37
NC_000001.9:g.157950113del	NCBI36
NG_013007.1:g.5892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000255030.9:c.502del MANE Select	ENSP00000255030.5:p.Gln168SerfsTer10
ENST00000368110.1:c.194-58del	ENSP00000357091.1:n.194-58del
ENST00000368111.5:c.194-58del	ENSP00000357092.1:n.194-58del
ENST00000368112.5:c.198-95del	ENSP00000357093.1:n.198-95del
ENST00000437342.1:c.-33del	ENSP00000402788.1:n.-33del
ENST00000473196.1:n.70del
ENST00000489317.1:n.74+309del
NM_000567.2:c.502del	NP_000558.2:p.Gln168SerfsTer10
XM_011509207.1:c.502del	XP_011507509.1:p.Gln168SerfsTer10
NM_001329057.1:c.502del	NP_001315986.1:p.Gln168SerfsTer10
NM_001329058.1:c.198-95del	NP_001315987.1:n.198-95del
NM_000567.3:c.502del MANE Select	NP_000558.2:p.Gln168SerfsTer10
NM_001329057.2:c.502del	NP_001315986.1:p.Gln168SerfsTer10
NM_001329058.2:c.198-95del	NP_001315987.1:n.198-95del
NM_001382703.1:c.194-58del	NP_001369632.1:n.194-58del